Yu-ichi Goto

3.2k total citations · 1 hit paper
39 papers, 2.1k citations indexed

About

Yu-ichi Goto is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Yu-ichi Goto has authored 39 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Yu-ichi Goto's work include Mitochondrial Function and Pathology (23 papers), Metabolism and Genetic Disorders (13 papers) and ATP Synthase and ATPases Research (12 papers). Yu-ichi Goto is often cited by papers focused on Mitochondrial Function and Pathology (23 papers), Metabolism and Genetic Disorders (13 papers) and ATP Synthase and ATPases Research (12 papers). Yu-ichi Goto collaborates with scholars based in Japan, United States and Australia. Yu-ichi Goto's co-authors include Yuichi Matsushima, Laurie S. Kaguni, Ikuya Nonaka, Satoshi O. Suzuki, Hidenori Otera, Hidetaka Morinaga, Sadaki Yokota, Ryoichi Takayanagi, Maki Maeda and Masatoshi Nomura and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Nature Cell Biology.

In The Last Decade

Yu-ichi Goto

39 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice

2009 849 citations Naotada Ishihara, Masatoshi Nomura et al. Nature Cell Biology profile →

Peers

Countries citing papers authored by Yu-ichi Goto

Since Specialization

Citations

This map shows the geographic impact of Yu-ichi Goto's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yu-ichi Goto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yu-ichi Goto more than expected).

Fields of papers citing papers by Yu-ichi Goto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yu-ichi Goto. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yu-ichi Goto. The network helps show where Yu-ichi Goto may publish in the future.

Co-authorship network of co-authors of Yu-ichi Goto

This figure shows the co-authorship network connecting the top 25 collaborators of Yu-ichi Goto. A scholar is included among the top collaborators of Yu-ichi Goto based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yu-ichi Goto. Yu-ichi Goto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Substitutions of nucleotides at the 3′ ends of COL6A1/2/3 exons induce exon skipping associated with collagen VI-related muscular dystrophies and therapeutic strategies 2025 ·Genetics in Medicine ·(unknown), Megumu Ogawa, Yoshihiko Saito, (unknown), Tomonari Awaya, (unknown), (unknown), (unknown), Akihide Takeuchi, (unknown), Yu-ichi Goto, Masatoshi Hagiwara, Ichizo Nishino, S. Noguchi	1
2	A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature 2019 ·Molecular Case Studies ·Aritoshi Iida, Kyoko Takano, Eri Takeshita, (unknown), Shinichi Hirabayashi, Yuji Inaba, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Ken Inoue, Yu-ichi Goto	8
3	A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation 2018 ·Human Genome Variation ·Aritoshi Iida, Eri Takeshita, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Kenji Kurosawa, Ken Inoue, Yu-ichi Goto	5
4	Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case report 2017 ·BMC Neurology ·(unknown), Kenji Fukuda, Tomonaga Matsushita, Yoshihisa Fukushima, Ryu Matsuo, Yu-ichi Goto, Takehiro Yasukawa, Takeshi Uchiumi, Dongchon Kang, Takanari Kitazono, Tetsuro Ago	11
5	Low dose resveratrol ameliorates mitochondrial respiratory dysfunction and enhances cellular reprogramming 2017 ·Mitochondrion ·(unknown), Hideyuki Hatakeyama, Kou Sueoka, Mamoru Tanaka, Yu-ichi Goto	30
6	Plasma Metabolites Predict Severity of Depression and Suicidal Ideation in Psychiatric Patients-A Multicenter Pilot Analysis 2016 ·PLoS ONE ·Daiki Setoyama, Takahiro A. Kato, Ryota Hashimoto, Hiroshi Kunugi, Kotaro Hattori, Kohei Hayakawa, Mina Sato‐Kasai, Norihiro Shimokawa, Sachie Kaneko, Sumiko Yoshida, Yu-ichi Goto, Yuka Yasuda, Hidenaga Yamamori, Masahiro Ohgidani, Noriaki Sagata, Daisuke Miura, Dongchon Kang, Shigenobu Kanba	98
7	Artificial oxygen carriers rescue placental hypoxia and improve fetal development in the rat pre-eclampsia model 2015 ·Scientific Reports ·Heng Li, Hidenobu Ohta, Yu Tahara, (unknown), Kazuaki Taguchi, Machiko Nakagawa, (unknown), Yu-ichi Goto, Keiji Wada, Makiko Kaga, Masumi Inagaki, Masaki Otagiri, Hideo Yokota, Shigenobu Shibata, Hiromi Sakai, Kunihiro Okamura, Nobuo Yaegashi	39
8	A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation 2014 ·Journal of Human Genetics ·Hirotomo Saitsu, Jun Tohyama, Tom Walsh, Mitsuhiro Kato, Yu Kobayashi, Ming Lee, Yoshinori Tsurusaki, Noriko Miyake, Yu-ichi Goto, Ichizo Nishino, Akira Ohtake, Mary‐Claire King, Naomichi Matsumoto	43
9	In vitro circadian period is associated with circadian/sleep preference 2013 ·Scientific Reports ·Akiko Hida, Shingo Kitamura, (unknown), Minori Enomoto, Yasuko Katayose, Yuki Motomura, Yoshiya Moriguchi, (unknown), Makiko Watanabe, Sayaka Aritake, Shigekazu Higuchi, Mie Kato, Yuichi Kamei, Shin Yamazaki, Yu-ichi Goto, Masaaki Ikeda, Kazuo Mishima	43
10	Effect of curcumin in a mouse model of Pelizaeus–Merzbacher disease 2012 ·Molecular Genetics and Metabolism ·(unknown), Toshifumi Morimura, (unknown), Ryoko Yamamoto, Naoko Inoue, (unknown), Yu-ichi Goto, Kimiko Deguchi, Hitoshi Osaka, Ken Inoue	21
11	Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice breakdown → 2009 ·Nature Cell Biology ·Naotada Ishihara, Masatoshi Nomura, (unknown), Hiroki Kato, Satoshi O. Suzuki, Keiji Masuda, Hidenori Otera, (unknown), Ikuya Nonaka, Yu-ichi Goto, (unknown), Hidetaka Morinaga, Maki Maeda, Ryoichi Takayanagi, Sadaki Yokota, Katsuyoshi Mihara	849
12	The development of novel quantification assay for mitochondrial DNA heteroplasmy aimed at preimplantation genetic diagnosis of Leigh encephalopathy 2007 ·Journal of Assisted Reproduction and Genetics ·Hiroto Tajima, Kou Sueoka, (unknown), (unknown), (unknown), (unknown), Hiroyoshi Watanabe, (unknown), (unknown), Shingo Kato, Yu-ichi Goto, Yasunori Yoshimura	19
13	A novel mtDNA C11777A mutation in Leigh syndrome 2003 ·Mitochondrion ·Hirofumi Komaki, Jun Akanuma, Hideki Iwata, Takao Takahashi, Yukihiko Mashima, Ikuya Nonaka, Yu-ichi Goto	43
14	Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene 2002 ·Neuromuscular Disorders ·Tatsuya Yamasoba, Yu-ichi Goto, Yoshitomo Oka, Ichizo Nishino, Katsunori Tsukuda, Ikuya Nonaka	14
15	Apoptosis is suspended in muscle of mitochondrial encephalomyopathies 2002 ·Acta Neuropathologica ·Koji Ikezoe, Masahiro Nakagawa, Chuanzhu Yan, Jun‐ichi Kira, Yu-ichi Goto, Ikuya Nonaka	34
16	Imprinting of Human GRB10 and Its Mutations in Two Patients with Russell-Silver Syndrome 2000 ·The American Journal of Human Genetics ·Hiroshi Yoshihashi, (unknown), Rika Kosaki, Tsutomu Ogata, Masato Tsukahara, Yu-ichi Goto, Jun-ichi Hata, Nobutake Matsuo, Robert J. Smith, Kenjiro Kosaki	69
17	Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder 2000 ·Molecular Psychiatry ·Kenjiro Kosaki, Taichi A. Suzuki, Rika Kosaki, Hiroshi Yoshihashi, Masayuki Itoh, Yu-ichi Goto, Naoki Matsuo	12
18	Localization of a Gene for Benign Adult Familial Myoclonic Epilepsy to Chromosome 8q23.3-q24.1 1999 ·The American Journal of Human Genetics ·Masaaki Mikami, Takeshi Yasuda, Akira Terao, Masayuki Nakamura, Shuichi Ueno, Hirotaka Tanabe, Toshihiro Tanaka, Teiichi Onuma, Yu-ichi Goto, Sunao Kaneko, Akira Sano	113
19	Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2 1997 ·Brain and Development ·Junko Tanaka, Toshisaburo Nagai, Hiroshi Arai, Koji Inui, Hideo Yamanouchi, Yu-ichi Goto, Ikuya Nonaka, Shintaro Okada	32
20	Detection of DNA Fragments Encompassing the Deletion Junction of Mitochondrial Genome 1996 ·Biochemical and Biophysical Research Communications ·Yu-ichi Goto, Ichizo Nishino, Satoshi Horai, Ikuya Nonaka	12

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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